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Results: 1-8 |
Results: 8
pH-independent hydrolysis of 4-nitrophenyl 2,2-dichloropropionate in aqueous micellar solutions: relative contributions of hydrophobic and electrostatic interactions
Authors: El Seoud, OA Ruasse, MF Possidonio, S
Citation: Oa. El Seoud et al., pH-independent hydrolysis of 4-nitrophenyl 2,2-dichloropropionate in aqueous micellar solutions: relative contributions of hydrophobic and electrostatic interactions, J PHYS ORG, 14(8), 2001, pp. 526-532
Optimization of micellar catalysis of nucleophilic substitution reactions in buffered solutions of cetyltrimethylammonium halide surfactants, part 2:buffers in the pH range 7-8
Authors: Ouarti, N Blagoeva, IB El Seoud, OA Ruasse, MF
Citation: N. Ouarti et al., Optimization of micellar catalysis of nucleophilic substitution reactions in buffered solutions of cetyltrimethylammonium halide surfactants, part 2:buffers in the pH range 7-8, J PHYS ORG, 14(11), 2001, pp. 823-831
Changes in the relative contribution of specific and general base catalysis in cationic micelles. The cyclization of substituted ethyl hydantoates
Authors: Blagoeva, IB Toteva, MM Ouarti, N Ruasse, MF
Citation: Ib. Blagoeva et al., Changes in the relative contribution of specific and general base catalysis in cationic micelles. The cyclization of substituted ethyl hydantoates, J ORG CHEM, 66(6), 2001, pp. 2123-2130
Hydrogen peroxide oxidation of mustard-model sulfides catalyzed by iron and manganese tetraarylporphyrines. Oxygen transfer to sulfides versus H2O2 dismutation and catalyst breakdown
Authors: Marques, A Marin, M Ruasse, MF
Citation: A. Marques et al., Hydrogen peroxide oxidation of mustard-model sulfides catalyzed by iron and manganese tetraarylporphyrines. Oxygen transfer to sulfides versus H2O2 dismutation and catalyst breakdown, J ORG CHEM, 66(23), 2001, pp. 7588-7595
Organic reactivity special issue - Preface
Authors: Siehl, HU Ruasse, MF
Citation: Hu. Siehl et Mf. Ruasse, Organic reactivity special issue - Preface, J PHYS ORG, 13(10), 2000, pp. 559-559
Optimization of micellar catalysis of nucleophilic substitutions in buffered cetyltrimethylammonium salt solutions. 1. Buffers for the 9-10 pH range
Authors: Ouarti, N Marques, A Blagoeva, I Ruasse, MF
Citation: N. Ouarti et al., Optimization of micellar catalysis of nucleophilic substitutions in buffered cetyltrimethylammonium salt solutions. 1. Buffers for the 9-10 pH range, LANGMUIR, 16(5), 2000, pp. 2157-2163
Substituent dependence of the diastereofacial selectivity in iodination and bromination of glycals and related cyclic enol ethers
Authors: Boschi, A Chiappe, C De Rubertis, A Ruasse, MF
Citation: A. Boschi et al., Substituent dependence of the diastereofacial selectivity in iodination and bromination of glycals and related cyclic enol ethers, J ORG CHEM, 65(25), 2000, pp. 8470-8477
Bromine-AOT charge-transfer complexes and hydrogen-bond donor ability of water in AOT-isooctane-H2O reverse micelles and water-in-oil microemulsions
Authors: Garcia-Rio, L Mejuto, JC Ciri, R Blagoeva, IB Leis, JR Ruasse, MF
Citation: L. Garcia-rio et al., Bromine-AOT charge-transfer complexes and hydrogen-bond donor ability of water in AOT-isooctane-H2O reverse micelles and water-in-oil microemulsions, J PHYS CH B, 103(24), 1999, pp. 4997-5004
Risultati: 1-8 |